Issue Information

Issue Information
Publié: (2024)

Issue Information
Publié: (2024)

Issue Information
Publié: (2024)

Issue Information
Publié: (2026)

Issue Information
Publié: (2025)

Issue Information
Publié: (2025)

Issue Information
Publié: (2025)

Issue Information
Publié: (2025)

Issue Information
Publié: (2026)

Issue Information
Publié: (2026)

Issue Information
Publié: (2025)

Issue Information
Publié: (2026)

Issue Information
Publié: (2025)

Issue Information
Publié: (2025)

Issue Information
Publié: (2025)

Issue Information
Publié: (2025)

Issue Information
Publié: (2025)

Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort
par: Dana Brabbing‐Goldstein, et autres
Publié: (2024)

Prenatal Screening Via cfDNA – Paired‐End Sequencing Utilizing Fragment Size Information Reduces the Screen Positive Rate for X Chromosome Aneuploidies
par: Susan Hancock, et autres
Publié: (2026)

Has the introduction of increased genetic prenatal testing affected rates of termination of pregnancy due to fetal abnormality?
par: Line Raaby, et autres
Publié: (2024)

Test performance and clinical utility of expanded non‐invasive prenatal test: Experience on 71,883 unselected routine cases from one single center
par: Monica Faieta, et autres
Publié: (2024)

Predictors of fetal death, neonatal survival and neurological outcomes in severe twin‐twin transfusion syndrome treated by laser ablation of placental vessels
par: Cleisson Fábio Andrioli Peralta, et autres
Publié: (2024)

Mammalian target of rapamycin inhibitors: A new‐possible approach for in‐utero medication therapy
par: Shohra Qaderi, et autres
Publié: (2024)

Caudal regression in fetus with de novo SMARCA2 pathogenic variant
par: Michelle Joy Wang, et autres
Publié: (2024)

Maternal cell contamination in postnatal umbilical cord blood samples implies a low risk for genetic misdiagnoses
par: Sanne P. Smeekens, et autres
Publié: (2024)

Noninvasive twin genotyping for recessive monogenic disorders by relative haplotype dosage
par: Lingrong Kong, et autres
Publié: (2024)

Clinical Characteristics and Outcomes of Intrauterine Blood Transfusion (IUT) for Infectious Etiologies
par: Jessian L. Munoz, et autres
Publié: (2024)

Maternal Vascular Malperfusion and Anatomic Cord Abnormalities Are Prevalent in Pregnancies With Fetal Congenital Heart Disease
par: Chrystalle Katte Carreon, et autres
Publié: (2024)

Is there an increased risk of genetic abnormalities in fetuses with congenital heart disease in the setting of growth restriction?
par: Kathleen Gianforcaro, et autres
Publié: (2024)

Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions
par: Brian Burnett, et autres
Publié: (2024)

The Conundrum of Mechanics Versus Genetics in Congenital Hydrocephalus and Its Implications for Fetal Therapy Approaches: A Scoping Review
par: Akos Herzeg, et autres
Publié: (2024)

The Association of Prenatal Alcohol Exposure With Brain Development During the First 1000 Days of Life: A Systematic Review
par: Marin Pielage, et autres
Publié: (2024)

A novel MED12 pathogenic variant in a female fetus with facial cleft and cardiac defects identified in the first trimester
par: Wei‐Si Dai, et autres
Publié: (2024)

Fetoscopic Release of Amniotic Bands Based on the Evidence—A Systematic Review
par: Fernando Ferrer‐Marquez, et autres
Publié: (2024)

Follow‐Up of Infants With Congenital Cytomegalovirus Following Maternal Primary Infection in the First Trimester and Normal Fetal Brain Imaging at Midgestation
par: Anna Seidenari, et autres
Publié: (2024)

Post‐Abortem Detection of a Pathogenic Somatic PIK3CA‐Variant in an Abdominal Lymphangioma That Is Not Present in Cultured Amniotic Fluid Cells
par: Cristiana Roggia, et autres
Publié: (2024)